Senior Global Safety Specialist
at Orifarm GmbH
5260 Odense, Region Syddanmark, Denmark -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 28 Jul, 2024 | Not Specified | 17 Jun, 2024 | N/A | Good communication skills | No | No |
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Description:
Ensuring the safety of post-marketed medicinal products within a dynamic team environment.
Do you enjoy flexibility in your work life and value the possibility of hybrid work? Do you have great competencies in signal management, aggregate reporting, and compliance tracking within the Global Safety Surveillance team? And do you thrive in a collaborative and fast-paced environment? Then this might just be the perfect role for you.
ABOUT ORIFARM
Everyone should have access to modern medicine. High costs or lack of access to pharmaceuticals should never impact our possibility to receive treatment or relief and live a healthy life. In Orifarm, we aim to bring healthy days by making modern healthcare a better deal for the people and the societies we serve. Working towards our vision, we create access to affordable high-quality pharmaceuticals and healthcare products by challenging markets and always seeking new opportunities. With our core values paving the way, we always act responsibly and constantly with our customers in the center of our attention. And everything we do is driven by our sole purpose:
For as many as possible, as healthy a day as possible.
Our history goes back to 1994 where Orifarm was founded in Denmark by Hans and Birgitte Bøgh-Sørensen. Since then, Orifarm has grown from a small nine-person company into an international company operating globally in 13 countries. Today, Orifarm is Europe’s largest parallel importer of pharmaceuticals and Denmark’s largest supplier of pharmaceuticals with more than 2,200 employees.
We operate within seven different business areas: Over the Counter (OTC), Consumer Healthcare, Generics, Promotional Rx, Unlicensed Medicines, Parallel Import and Clinical Trials Supplies (CTS). Further, we focus heavily on new business opportunities and synergistic M&A to expand our offerings
NEED FURTHER INFORMATION?
If you need further information about the job, please contact either:
- Sarah Rohde Friis, Department Manager, Global Safety Surveillance, at sarra@orifarm.com
- Maria Harritsø Wolff, Director, Global Safety & EU/UK QPPV, at mawol@orifarm.com
We are often looking for new employees to help us grow and therefore, we may have other interesting opportunities for you. Follow us on LinkedIn to receive updates on our business activities and job opportunities: https://www.linkedin.com/feed/
Responsibilities:
- Signal Management activities
- Aggregate Reporting activities
- Interacting with competent authorities
- Extraction and analysis of pharmacovigilance data
- Overseeing vendor literature monitoring
- Strong cooperation with other departments, stakeholders and affiliates
- Promoting, maintaining, and improving compliance with the legal requirements in the EU
- Leading tasks/projects within the team and ensuring that deadlines are met
- Contribute to the ongoing globalizatio
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
5260 Odense, Denmark